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Human Disease and Mouse Model Detail
Human Disease Epilepsy, Familial Adult Myoclonic, 2; FAME2
OMIM ID: 607876
Human Phenotype Ontology associations
Synonyms Benign Adult Familial Myoclonic Epilepsy 2; BAFME2; Cortical Myoclonic Tremor with Epilepsy, Familial, 2; FCMTE2; Cortical Myoclonus and Epilepsy, Autosomal Dominant; ADCME; Epilepsy, Familial Adult Myoclonic
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ADRA2B* Adra2b   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory